ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.767C>G (p.Ser256Cys)

dbSNP: rs2143852373
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001371561 SCV001568131 uncertain significance Fanconi anemia complementation group O 2022-09-19 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt RAD51C protein function. This sequence change replaces serine, which is neutral and polar, with cysteine, which is neutral and slightly polar, at codon 256 of the RAD51C protein (p.Ser256Cys). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with RAD51C-related conditions. ClinVar contains an entry for this variant (Variation ID: 1061903).

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